Home Nitro Compounds 2042-14-0
2042-14-0,MFCD00007244
Catalog No.:AA00299H

2042-14-0 | 4-Methyl-3-nitrophenol

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5g
98%
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$6.00   $4.00
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10g
98%
in stock  
$7.00   $5.00
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25g
98%
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$14.00   $10.00
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100g
98%
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$50.00   $35.00
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500g
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$245.00   $171.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00299H
Chemical Name:
4-Methyl-3-nitrophenol
CAS Number:
2042-14-0
Molecular Formula:
C7H7NO3
Molecular Weight:
153.1354
MDL Number:
MFCD00007244
SMILES:
Oc1ccc(c(c1)[N+](=O)[O-])C
NSC Number:
41205
Properties
Properties
 
BP:
276°C at 760 mmHg  
Form:
Solid  
MP:
78-81 °C  
Refractive Index:
1.5744 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
154  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
XLogP3:
2.1  

Upstream Synthesis Route

[1]BioorganicandMedicinalChemistryLetters,2013,vol.23,#13,p.3942-3946

[1]JournaloftheChemicalSociety,1921,vol.119,p.1612

[2]JournaloftheChemicalSociety,1922,vol.121,p.1872

[1]Tetrahedron,1996,vol.52,#24,p.8099-8112

[2]JournaloftheChemicalSociety,1937,p.1726

[3]JournaloftheChemicalSociety,1937,p.1726

[1]JournaloftheChemicalSociety,1929,p.252

[2]Tetrahedron,2018,vol.74,#12,p.1294-1306

[1]EuropeanJournalofMedicinalChemistry,2018,vol.157,p.380-396

Downstream Synthesis Route

[1]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.240-244

[2]GreenChemistry,2017,vol.19,p.809-815

[3]JournalofMedicinalChemistry,2010,vol.53,p.1964-1978

[4]ACSCatalysis,2017,vol.7,p.2412-2418

[5]Patent:WO2018/208132,2018,A1.Locationinpatent:Paragraph704-708

[6]AngewandteChemie-InternationalEdition,2016,vol.55,p.8979-8983    Angew.Chem.,2016,vol.128,p.9125-9129,5

[7]Patent:WO2017/106426,2017,A1.Locationinpatent:Paragraph0084;0087

[8]JustusLiebigsAnnalenderChemie,1882,vol.215,p.83

[9]JournaloftheChemicalSociety,1929,p.252

[10]CanadianJournalofChemistry,1955,vol.33,p.1819,1822

[11]JournalofgeneralchemistryoftheUSSR,1960,vol.30,p.3374-3379    ZhurnalObshcheiKhimii,1960,vol.30,p.3407-3412

[12]JournaloftheAmericanChemicalSociety,2005,vol.127,p.10545-10559

[13]Patent:US4345077,1982,A

[14]Patent:WO2014/145022,2014,A1.Locationinpatent:Page/Pagecolumn53

[15]ChemCatChem,2016,vol.8,p.1485-1489

[16]ChemicalCommunications,2016,vol.52,p.9442-9445

[17]ChemCatChem,2017,vol.9,p.3743-3751

[18]RSCAdvances,2018,vol.8,p.8898-8909

[19]AppliedCatalysisA:General,2018,vol.559,p.127-137

[1]Patent:WO2014/149164,2014,A1.Locationinpatent:Paragraph00995

[2]JournaloftheChemicalSociety,1927,p.586

[1]Tetrahedron,1996,vol.52,p.8099-8112

[2]JournalofOrganicChemistry,2010,vol.75,p.2785-2789

[3]JournaloftheChemicalSociety,1937,p.1726

[4]BulletindelaSocieteChimiquedeFrance,1972,p.4722-4731

[1]Synthesis,1986,p.735-737

[2]CanadianJournalofChemistry,1987,vol.65,p.1233-1240

[3]JournaloftheChemicalSociety,1929,p.252

[4]JournaloftheChemicalSociety,1921,vol.119,p.1612    JournaloftheChemicalSociety,1922,vol.121,p.1872

[5]HelveticaChimicaActa,1932,vol.15,p.394,402

[6]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1937,vol.57,p.992,995;dtsch.Ref.S.274,277    Chem.Abstr.,1938,p.2519

[7]MonatsheftefurChemie,1960,vol.91,p.1152-1161

[1]Chemistry-AEuropeanJournal,2009,vol.15,p.2742-2746

[2]Patent:WO2016/128541,2016,A1.Locationinpatent:Page/Pagecolumn92;93

[3]Patent:WO2017/162834,2017,A1.Locationinpatent:Page/Pagecolumn85

[4]EuropeanJournalofMedicinalChemistry,2020,vol.200

[5]ChemMedChem,2019,vol.14,p.2005-2022

[6]JustusLiebigsAnnalenderChemie,1882,vol.215,p.83

[7]JournalofgeneralchemistryoftheUSSR,1960,vol.30,p.3374-3379    ZhurnalObshcheiKhimii,1960,vol.30,p.3407-3412

[8]JournalofgeneralchemistryoftheUSSR,1960,vol.30,p.3091-3095    ZhurnalObshcheiKhimii,1960,vol.30,p.3118

[9]Tetrahedron,1992,vol.48,p.2919-2924

Literature
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SDS
Tags:2042-14-0 Molecular Formula|2042-14-0 MDL|2042-14-0 SMILES|2042-14-0 4-Methyl-3-nitrophenol